Europese Unie - Nederlands - EMA (European Medicines Agency)

ipsen pharma - cabozantinib - schildklierneoplasma - antineoplastische middelen - behandeling van volwassen patiënten met progressief, niet-reseceerbaar lokaal gevorderd of gemetastaseerd medullair schildkliercarcinoom.

Europese Unie - Nederlands - EMA (European Medicines Agency)

ipsen pharma - cabozantinib (s)-malate - carcinoma, renal cell; carcinomas, hepatocellular - antineoplastische middelen - renal cell carcinoma (rcc)cabometyx is indicated as monotherapy for the treatment of advanced renal cell carcinoma (rcc):in treatment-naïve adults with intermediate or poor risk,in adults following prior vascular endothelial growth factor (vegf)-targeted therapy. cabometyx, in combination with nivolumab, is indicated for the first-line treatment of advanced renal cell carcinoma in adults. hepatocellular carcinoma (hcc)cabometyx is indicated as monotherapy for the treatment of hepatocellular carcinoma (hcc) in adults who have previously been treated with sorafenib.

Europese Unie - Nederlands - EMA (European Medicines Agency)

deciphera pharmaceuticals (netherlands) b.v. - ripretinib - gastro-intestinale stromale tumoren - antineoplastische middelen - qinlock is indicated for the treatment of adult patients with advanced gastrointestinal stromal tumour (gist) who have received prior treatment with three or more kinase inhibitors, including imatinib.

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

sandoz b.v. veluwezoom 22 1327 ah almere - erlotinibhydrochloride 109,3 mg/stuk samenstelling overeenkomend met ; erlotinib 100 mg/stuk - filmomhulde tablet - cellulose, microkristallijn (e 460) ; copolymeer van ethylacrylaat-methacrylzuur (1:1) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumwaterstofcarbonaat (e 500 (ii)) ; natriumzetmeelglycolaat ; polyvinylalcohol (e1203) ; talk (e 553 b) ; titaandioxide (e 171), cellulose, microkristallijn (e 460) ; copolymeer van ethylacrylaat-methacrylzuur (1:1) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumwaterstofcarbonaat (e 500 (ii)) ; natriumzetmeelglycolaat (e468) ; polyvinylalcohol (e1203) ; talk (e 553 b) ; titaandioxide (e 171) - erlotinib

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

sandoz b.v. veluwezoom 22 1327 ah almere - erlotinibhydrochloride 163,9 mg/stuk samenstelling overeenkomend met ; erlotinib 150 mg/stuk - filmomhulde tablet - cellulose, microkristallijn (e 460) ; copolymeer van ethylacrylaat-methacrylzuur (1:1) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumwaterstofcarbonaat (e 500 (ii)) ; natriumzetmeelglycolaat ; polyvinylalcohol (e1203) ; talk (e 553 b) ; titaandioxide (e 171), cellulose, microkristallijn (e 460) ; copolymeer van ethylacrylaat-methacrylzuur (1:1) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumwaterstofcarbonaat (e 500 (ii)) ; natriumzetmeelglycolaat (e468) ; polyvinylalcohol (e1203) ; talk (e 553 b) ; titaandioxide (e 171) - erlotinib

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

sandoz b.v. veluwezoom 22 1327 ah almere - erlotinibhydrochloride 27,3 mg/stuk samenstelling overeenkomend met ; erlotinib 25 mg/stuk - filmomhulde tablet - cellulose, microkristallijn (e 460) ; copolymeer van ethylacrylaat-methacrylzuur (1:1) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumwaterstofcarbonaat (e 500 (ii)) ; natriumzetmeelglycolaat ; polyvinylalcohol (e1203) ; talk (e 553 b) ; titaandioxide (e 171), cellulose, microkristallijn (e 460) ; copolymeer van ethylacrylaat-methacrylzuur (1:1) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumwaterstofcarbonaat (e 500 (ii)) ; natriumzetmeelglycolaat (e468) ; polyvinylalcohol (e1203) ; talk (e 553 b) ; titaandioxide (e 171) - erlotinib

Europese Unie - Nederlands - EMA (European Medicines Agency)

eisai gmbh - lenvatinib mesilaat - carcinoom, niercel - antineoplastische middelen - kisplyx is indicated for the treatment of adults with advanced renal cell carcinoma (rcc):in combination with pembrolizumab, as first-line treatment (see section 5. in combination with everolimus, following one prior vascular endothelial growth factor (vegf)-targeted therapy.

Europese Unie - Nederlands - EMA (European Medicines Agency)

accord healthcare s.l.u. - doxorubicin hydrochloride, liposomal - ovarian neoplasms; sarcoma, kaposi; multiple myeloma - doxorubicin - zolsketil pegylated liposomal is a medicine used to treat the following types of cancer in adults:• breast cancer that has spread to other parts of the body in patients at risk of heart problems. zolsketil pegylated liposomal is used on its own for this disease;• advanced ovarian cancer in women whose previous treatment including a platinum-based cancer medicine has stopped working;• multiple myeloma (a cancer of the white blood cells in the bone marrow), in patients with progressive disease who have received at least one other treatment in the past and have already had, or are unsuitable for, a bone marrow transplantation. zolsketil pegylated liposomal is used in combination with bortezomib (another cancer medicine);• kaposi’s sarcoma in patients with aids who have a very damaged immune system. kaposi’s sarcoma is a cancer that causes abnormal tissue to grow under the skin, on moist body surfaces or on internal organs. zolsketil pegylated liposomal contains the active substance doxorubicin and is a ‘hybrid medicine’. this means that it is similar to a ‘reference medicine’ containing the same active substance called adriamycin. however, in zolsketil pegylated liposomal the active substance is enclosed in tiny fatty spheres called liposomes, whereas this is not the case for adriamycin.

Europese Unie - Nederlands - EMA (European Medicines Agency)

yes pharmaceutical development services gmbh - doxorubicine hydrochloride - breast neoplasms; ovarian neoplasms; multiple myeloma; sarcoma, kaposi - antineoplastische middelen - celdoxome pegylated liposomal is indicated in adults:as monotherapy for patients with metastatic breast cancer, where there is an increased cardiac risk. or treatment of advanced ovarian cancer in women who have failed a first-line platinum-based chemotherapy regimen. in combination with bortezomib for the treatment of progressive multiple myeloma in patients who have received at least one prior therapy and who have already undergone or are unsuitable for bone marrow transplant. for treatment of aids-related kaposi’s sarcoma (ks) in patients with low cd4 counts (< 200 cd4 lymphocytes/mm3) and extensive mucocutaneous or visceral disease. celdoxome pegylated liposomal may be used as first-line systemic chemotherapy, or as second line chemotherapy in aids-ks patients with disease that has progressed with, or in patients intolerant to, prior combination systemic chemotherapy comprising at least two of the following agents: a vinca alkaloid, bleomycin and standard doxorubicin (or other anthracycline).

Europese Unie - Nederlands - EMA (European Medicines Agency)

accord healthcare s.l.u. - sunitinib - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - antineoplastische middelen - gastrointestinal stromal tumour (gist)sunitinib accord is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sunitinib accord is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sunitinib accord is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours (pnet) with disease progression in adults.